Losartan Potassium
Product Images NDC 60760-645

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 60760-645). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

645 (Losartan 645 30)

645 (Losartan 645 30)
NDC 60760-645-30 is a tablets medication called Losartan that includes potassium - manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd, China. The tablets contain 50mg Potassium and the package size is 30 tablets. Additionally, it includes LOT# and EXP date for product identification. The medication is for prescription use only, and should be stored at temperatures between 15°C-30°C (59°F-86°F). If any further details on the medication are required, please refer to Use as Directed at the given website.*
FDA Label Image

Chemical Structure (Spl Image1 Structure1)

FDA Label Image

Figure 1 (Spl Image2 Figure1)

Figure 1 (Spl Image2 Figure1)
The text provides information about a study where the drug Atenolol was compared with Losartan Potassium in patients. The primary endpoint was measured as the percentage of patients at a specific risk level, and the study was conducted over a period of 66 months. The risk reduction was found to be 13% with a significance level of p=0.021.*
FDA Label Image

Figure 2 (Spl Image3 Figure2)

Figure 2 (Spl Image3 Figure2)
This text seems to be presenting data about a comparison between two drugs: Atenolol and Losartan Potassium. It suggests that Losartan Potassium may have an adjusted risk reduction of 25% compared to Atenolol, with statistical significance (p=0.001). The text also appears to show percentages of patients with fatal/non-fatal strokes over the course of some study months, ranging from 6 to 66. However, without more context or clear headings, it is difficult to interpret the information fully.*
FDA Label Image

Figure 3 (Spl Image4 Figure3)

Figure 3 (Spl Image4 Figure3)
The text describes primary composite stroke events in demographic subgroups for a clinical trial comparing the effectiveness of Losartan Potassium and Atenolol. The trial studied the effects on patients with different age groups, gender, race, presence/absence of ischemic heart disease, diabetes, history of cardiovascular diseases. The text also mentions the hazard ratio and adjusted baseline risk of patients.*
FDA Label Image

Figure 4 (Spl Image5 Figure4)

Figure 4 (Spl Image5 Figure4)
This is a graph showing the percentage of patients experiencing an event over time. The graph compares the effects of Losartan Potassium versus a placebo, with Losartan Potassium showing a risk reduction of 16.1% and a p-value of 0.022. The x-axis shows the duration of the study in months.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.